@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_head
{
this:
np:hasAssertion
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_assertion
;
np:hasProvenance
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_provenance
;
np:hasPublicationInfo
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_assertion
a
np:Assertion
.
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_provenance
a
np:Provenance
.
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_assertion
{
miriam-gene:25830
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN2c25e3aab16131a1a83b4a079e32f2db
sio:SIO_000628
miriam-gene:25830
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_provenance
{
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_assertion
dcterms:description
"[We hypothesised that if functional dysregulation of SULT4A1 was involved in the aetiology of schizophrenia, then genetic variants in the coding sequence of SULT4A1 might be identified in cases compared with controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19125109
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP430701.RA2vft3-OpT-_lVjX8p7I7WZs9GxmeZE5lOUFbTo_9tQc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}